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Professur für Humangenetik
Friedrich-Alexander-Universität Erlangen-Nürnberg
Medizinische Fakultät
Einrichtungen, die zum Universitätsklinikum Erlangen gehören
Institute of Human Genetics
Lehrstuhl für Humangenetik
Overview
Publications
(28)
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Journal article
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Book chapter / Article in edited volumes
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Translation
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Hobit- and Blimp-1-driven CD4(+) tissue-resident memory T cells control chronic intestinal inflammation (2019)
Zundler S, Becker E, Spocinska M, Slawik M, Parga-Vidal L, Stark R, Wiendl M, et al.
Journal article
Inflammation-induced glycolytic switch controls suppressivity of mesenchymal stem cells via STAT1 glycosylation (2019)
Jitschin R, Böttcher M, Saul D, Lukassen S, Bruns H, Loschinski R, Ekici AB, et al.
Journal article
Pain relief in a neuropathy patient by lacosamide: Proof of principle of clinical translation from patient-specific iPS cell-derived nociceptors (2018)
Namer B, Schmidt D, Eberhardt E, Maroni M, Dorfmeister E, Kleggetveit IP, Kaluza L, et al.
Journal article
Single-cell RNA sequencing of adult mouse testes (2018)
Lukassen S, Bosch E, Ekici AB, Winterpacht A
Journal article
Chromatin-Remodeling Factor SPOC1 Acts as a Cellular Restriction Factor against Human Cytomegalovirus by Repressing the Major Immediate Early Promoter (2018)
Reichel A, Stilp AC, Scherer M, Reuter N, Lukassen S, Kasmapour B, Schreiner S, et al.
Journal article
Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing (2018)
Lukassen S, Bosch E, Ekici AB, Winterpacht A
Journal article
PEDF Is Associated with the Termination of Chondrocyte Phenotype and Catabolism of Cartilage Tissue (2017)
Klinger P, Lukassen S, Ferrazzi F, Ekici AB, Hotfiel T, Swoboda B, Aigner T, Gelse K
Journal article
Association of genetic and psychological factors with persistent pain after cosmetic thoracic surgery (2015)
Dimova V, Loetsch J, Hühne K, Winterpacht A, Heesen M, Parthum A, Weber PG, et al.
Journal article
Matrilin-1 is essential for zebrafish development by facilitating collagen II secretion (2014)
Neacsu CD, Ko YP, Tagariello A, Karlsen KR, Neiss WF, Paulsson M, Wagener R
Journal article
Inherited pain: sodium channel Nav1.7 A1632T mutation causes erythromelalgia due to a shift of fast inactivation (2014)
Eberhardt M, Nakajima J, Klinger A, Neacsu C, Hühne K, o' Reilly A, Kist A, et al.
Journal article
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